Multiple Carboxylase Deficiency Overview
Learn About Multiple Carboxylase Deficiency
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However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.
Optum Medical Care Of New Jersey PC
Prashant Pandya is an Internal Medicine provider in Bayonne, New Jersey. Dr. Pandya and is rated as an Experienced provider by MediFind in the treatment of Multiple Carboxylase Deficiency. His top areas of expertise are High Cholesterol, Obesity in Children, Hypothyroidism, and Macrophagic Myofasciitis. Dr. Pandya is currently accepting new patients.
Mmc Hematology Oncology Fpp
Yiqing Xu is a Hematologist Oncology specialist and a Hematologist in Brooklyn, New York. Dr. Xu and is rated as an Experienced provider by MediFind in the treatment of Multiple Carboxylase Deficiency. Her top areas of expertise are Pseudomyxoma Peritonei, Ovarian Carcinosarcoma, Virilizing Ovarian Tumor, Testicular Yolk Sac Tumor, and Splenectomy.
N.Z.S. Medical PC
Yefim Sosonkin is an Internal Medicine provider in Staten Island, New York. Dr. Sosonkin and is rated as an Advanced provider by MediFind in the treatment of Multiple Carboxylase Deficiency. His top areas of expertise are Vitamin B12 Deficiency Anemia, Folate Deficiency, Multiple Carboxylase Deficiency, and Anemia.
Summary: Newborn screening (NBS) is a global initiative of systematic testing at birth to identify babies with pre-defined severe but treatable conditions. With a simple blood test, rare genetic conditions can be easily detected, and the early start of transformative treatment will help avoid severe disabilities and increase the quality of life. Baby Detect Project is an innovative NBS program using a pane...
Summary: Retro-prospective, single-centre, observational study conducted at the Endocrine-Metabolic Diseases Center of the Pediatrics Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Italy. The study involves children born in Emilia-Romagna region, Italy, from January 2016 to December 2020 with biotinidase deficiency identified through Neontal Screening at the Endocrine-Metabolic Diseases Center o...